A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158735



Internal ID21452103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107053644..107053644hg38UCSC Ensembl
chr8:108065872..108065872hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637733
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158735
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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